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rs148000791

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs148000791(C;C)
Make rs148000791(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position135323233
GeneAHI1
is asnp
is mentioned by
dbSNPrs148000791
ebirs148000791
HLIrs148000791
Exacrs148000791
Varsomers148000791
Maprs148000791
PheGenIrs148000791
hapmaprs148000791
1000 genomesrs148000791
hgdprs148000791
ensemblrs148000791
gopubmedrs148000791
geneviewrs148000791
scholarrs148000791
googlers148000791
pharmgkbrs148000791
gwascentralrs148000791
openSNPrs148000791
23andMers148000791
23andMe allrs148000791
SNP Nexus

SNPshotrs148000791
SNPdbers148000791
MSV3drs148000791
GWAS Ctlgrs148000791
Max Magnitude0
ClinVar
Risk rs148000791(C;C)
Alt rs148000791(C;C)
Reference rs148000791(T;T)
Significance Other
Disease not provided Joubert syndrome 3
Variation info
Gene AHI1
CLNDBN not provided Joubert syndrome 3
Reversed 0
HGVS NC_000006.11:g.135644371T>C
CLNSRC
CLNACC RCV000132677.2, RCV000198715.1,